Original language | English (US) |
---|---|
Pages (from-to) | e377 |
Journal | Brain |
Volume | 138 |
Issue number | 9 |
DOIs | |
State | Published - Sep 1 2015 |
ASJC Scopus subject areas
- Clinical Neurology
Access to Document
Other files and links
Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS
Reply : A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. / Bannwarth, Sylvie; Ait-El-Mkadem, Samira; Chaussenot, Annabelle; Genin, Emmanuelle C.; Lacas-Gervais, Sandra; Fragaki, Konstantina; Berg-Alonso, Laetitia; Kageyama, Yusuke; Serre, Valérie; Moore, David; Verschueren, Annie; Rouzier, Cécile; Le Ber, Isabelle; Augé, Gaëlle; Cochaud, Charlotte; Lespinasse, Françoise; N'Guyen, Karine; De Septenville, Anne; Brice, Alexis; Yu-Wai-Man, Patrick; Sesaki, Hiromi; Pouget, Jean; Paquis-Flucklinger, Véronique.
In: Brain, Vol. 138, No. 9, 01.09.2015, p. e377.Research output: Contribution to journal › Letter › peer-review
}
TY - JOUR
T1 - Reply
T2 - A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation
AU - Bannwarth, Sylvie
AU - Ait-El-Mkadem, Samira
AU - Chaussenot, Annabelle
AU - Genin, Emmanuelle C.
AU - Lacas-Gervais, Sandra
AU - Fragaki, Konstantina
AU - Berg-Alonso, Laetitia
AU - Kageyama, Yusuke
AU - Serre, Valérie
AU - Moore, David
AU - Verschueren, Annie
AU - Rouzier, Cécile
AU - Le Ber, Isabelle
AU - Augé, Gaëlle
AU - Cochaud, Charlotte
AU - Lespinasse, Françoise
AU - N'Guyen, Karine
AU - De Septenville, Anne
AU - Brice, Alexis
AU - Yu-Wai-Man, Patrick
AU - Sesaki, Hiromi
AU - Pouget, Jean
AU - Paquis-Flucklinger, Véronique
PY - 2015/9/1
Y1 - 2015/9/1
UR - http://www.scopus.com/inward/record.url?scp=84926411806&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84926411806&partnerID=8YFLogxK
U2 - 10.1093/brain/awv015
DO - 10.1093/brain/awv015
M3 - Letter
C2 - 25681413
AN - SCOPUS:84926411806
VL - 138
SP - e377
JO - Brain
JF - Brain
SN - 0006-8950
IS - 9
ER -